Double-sided container capacitors are formed using sacrificial layers. A sacrificial layer is formed within a recess in a structural layer. A lower electrode is formed within the recess. The sacrificial layer is removed to create a space to allow access to the sides of the structural layer. The structural layer is removed, creating an isolated lower electrode. The lower electrode can be covered with a capacitor dielectric and upper electrode to form a double-sided container capacitor.
|
35. A method of forming a capacitor in an integrated circuit comprising
forming a sacrificial layer in a recess in a structural layer;
forming a lower electrode within the sacrificial layer;
doping a portion of the sacrificial layer, wherein doping creates a doped portion and an undoped portion; and
removing one of the doped portion and the undoped portion, wherein doping the portion of the sacrificial layer comprises forming a dopant collar within the structural layer.
31. A method of forming a capacitor in an integrated circuit compnsing
forming a sacrificial layer in a recess in a structural layer, the sacrificial layer having a thickness extending from an outer surface to an inner surface;
forming a lower electrode within the sacrificial layer;
doping a portion of the sacrificial layer, wherein doping creates a doped portion extending through the thickness and an undoped portion extending through the thickness; and
removing one of the doped portion and the undoped portion.
1. A method of forming an isolated lower electrode for a memory array, comprising:
depositing a sacrificial layer within a recess having a base and sidewalls in a structural layer material;
depositing a protective liner over the sacrificial layer;
removing the sacrificial layer and the protective liner from the base of the recess;
depositing a lower electrode within the sacrificial layer and protective layer in the recess;
etching the sacrificial layer within the recess after depositing the lower electrode;
removing the protective liner; and
removing the structural layer material from the memory array after etching the sacrificial layer.
11. A method of forming a capacitor for a dram memory cell comprising
forming a recess within a structural layer over an interlayer dielectric layer, wherein the recess has a base and sidewalls;
forming a sacrificial layer along the sidewalls of the recess;
forming a lower electrode within the sacrificial layer in the recess;
doping a portion of the sacrificial layer to form an etch stop;
removing the sacrificial layer above the etch stop after forming the lower electrode;
removing at least a portion of the structural layer after removing the sacrificial layer;
forming a conformal capacitor dielectric over the lower electrode after removing at least a portion of the structural layer; and
forming a conformal upper electrode over the conformal capacitor dielectric.
2. The method of
3. The method of
4. The method of
6. The method of
7. The method of
8. The method of
9. The method of
10. The method of
12. The method of
forming an oxide layer with a high concentration of a dopant within the structural layer;
allowing the dopant to diffuse into a layer of the sacrificial layer.
13. The method of
14. The method of
15. The method of
16. The method of
17. The method of
18. The method of
forming a metallic layer with a diffusing metal within the structural layer;
allowing the diffusing metal to diffuse into a layer of the sacrificial layer.
19. The method of
20. The method of
21. The method of
23. The method of
24. The method of
25. The method of
26. The method of
27. The method of
28. The method of
29. The method of
30. The method of
32. The method of
33. The method of
34. The method of
37. The method of
|
The present invention claims priority under 35 U.S.C. §119(e) to U.S. Provisional Application No. 60/607,365, filed Sep. 2, 2004, the entire disclosure of which is hereby incorporated by reference herein.
The present invention relates to the field of integrated circuit fabrication, specifically to the fabrication of capacitors.
Since the introduction of the digital computer, electronic storage devices have been a vital resource for the retention of data. Conventional semiconductor electronic storage devices typically incorporate capacitor and transistor structures, such as Dynamic Random Access Memory (DRAM), which temporarily store data based on the charged state of the capacitor structure. In general, this type of semiconductor Random Access Memory (RAM) often requires densely packed capacitor structures that are easily accessible for electrical interconnection. Many of these capacitor structures are fabricated with layers of material including semiconductor, dielectric, and metal.
Double-sided container capacitors are useful in DRAM circuits because they can be tightly packed. Additionally, overall capacitance of each capacitor is increased due to the high surface area including inside and outside surfaces of the container. Some of these structures have lower electrodes that are fabricated by first forming sacrificial spacers within a recess in a substrate, and then forming the lower electrode within the recess and lining annulus defined by the sacrificial layer on the sidewalls of the recess. An application describing this process was filed on Nov. 13, 2003, U.S. patent application Ser. No. 10/714,115. The selection of materials to be used for the lower electrode and the sacrificial layer can be important for cost and production purposes. Additionally, some sacrificial layers are not as effective as others in certain fabrication processes and when used with different materials. For this reason, additional methods of fabricating double-sided container capacitors are desirable.
In one aspect of the invention, a method is provided for forming an isolated lower electrode for a memory array. The method comprises depositing a sacrificial layer within a recess having a base and sidewalls in a structural layer material and depositing a protective liner over the sacrificial layer. The sacrificial layer and the protective liner are removed from the base of the recess and a lower electrode is deposited within the sacrificial layer and protective layer in the recess. The sacrificial layer is etched and the protective liner is removed. The method further comprises removing the structural layer from the memory array after etching the sacrificial layer.
In another aspect of the invention, a method of forming an electrically isolated capacitor electrode is disclosed. The method comprises creating a recess over a conductive contact plug in a structural layer and depositing a phosphosilicate glass (PSG) layer within the recess. The PSG layer is etched over the conductive contact plug and a container capacitor electrode is formed within the PSG layer in the recess. The method further comprises removing the PSG layer.
A method of forming a capacitor for a memory cell is disclosed in another aspect of the invention. The method comprises forming a recess within a structural layer and lining the sidewalls of the recess with a germanium oxide sacrificial layer. A lower electrode is deposited within the sacrificial layer and the sacrificial layer is removed from the sidewalls of the recess to form an access space. The structural layer is removed using an aqueous etchant in the access space. The method further comprises depositing a capacitor dielectric and an upper electrode conformally over the lower electrode.
In another aspect of the invention, a method of forming an isolated bottom capacitor electrode is disclosed. A recess is produced within a substantially undoped oxide structural layer and a doped oxide sacrificial liner is formed within the recess. A bottom electrode is deposited within the recess and the doped oxide sacrificial liner is etched selectively to the substantially undoped oxide structural layer. The substantially undoped oxide structural layer is removed.
A method of forming a capacitor for a memory cell is disclosed in another aspect of the invention. The method comprises forming a recess within a structural layer over an interlayer dielectric layer. A sacrificial layer is formed along the sidewalls of the recess and a lower electrode is formed within the sacrificial layer. A portion of the sacrificial layer is doped to form an etch stop. The sacrificial layer above the etch stop is removed. The structural layer is removed after the sacrificial layer is removed. A conformal capacitor dielectric is formed over the lower electrode and a conformal upper electrode is formed over the conformal capacitor dielectric.
In another aspect of the invention, a capacitor array for an integrated circuit is disclosed. The array comprises a plurality of conductive contact plugs within an interlayer dielectric layer and a plurality of container-shaped lower electrodes over each conductive plug. An insulating layer is positioned between the lower electrodes and an electrically unconnected metallic layer is over a portion of the insulating layer. A conformal capacitor dielectric that isolates the metallic layer extends over the lower electrodes. An upper electrode extends conformally over the conformal capacitor dielectric.
In another aspect of the invention, an integrated circuit including a capacitor is provided. The capacitor comprises a conductive contact plug within an underlayer and a container-shaped lower electrode over and electrically connected to the conductive contact plug. A polysilicon stub is next to a portion of the lower electrode on the substrate and a conformal capacitor dielectric extends over the lower electrode and the polysilicon stub. An upper electrode extends conformally over the conformal capacitor dielectric.
A method of fabricating a capacitor array for integrated circuits is disclosed in another aspect of the invention. The method comprises providing an insulating structural layer over a substrate and forming a plurality of recesses within the structural layer. A sacrificial layer is formed within each recess and an insulating protective liner is provided conformally over each sacrificial layer. A conductive plug is exposed in each recess and a first electrode is formed within each sacrificial layer. At least a portion of each sacrificial layer is removed before the structural layer is etched by exposure to an aqueous etchant solution. A conformal dielectric layer is provided over the first electrode and a top electrode is formed over the conformal dielectric layer.
In another aspect, a method of forming a memory cell is disclosed. The method comprises forming a borosilicate glass layer with a high boron concentration within a structural layer over an interlayer dielectric. A recess is formed within the structural layer, and the recess's walls are lined with a polysilicon sacrificial layer. The borosilicate glass layer produces a p-doped etch stop layer within the polysilicon sacrificial layer by diffusion of boron. A metallic first container capacitor electrode is formed within the polysilicon sacrificial layer. The polysilicon sacrificial layer is removed above the etch stop layer to form access spaces. The structural layer is recessed by allowing an etchant access to the structural layer from the access spaces. A conformal capacitor dielectric is deposited over the first container capacitor and a top electrode is formed over the conformal capacitor dielectric to form an isolated capacitor. The method further comprises providing a connection to a transistor.
A method of forming a capacitor in an integrated circuit is disclosed in another aspect of the invention. The method comprises forming a sacrificial layer in a recess in a structural layer. A lower electrode is formed within the sacrificial layer. A portion of the sacrificial layer is doped so that there is a doped portion and an undoped portion of the sacrificial layer. The method further comprises removing either the doped portion or the undoped portion.
The formation of capacitors is critical to the functionality of dynamic random access memory (DRAM) cells. One form of a capacitor is a double-sided container capacitor, which uses a cup-shaped lower, or bottom, electrode with a conformal dielectric and a conformal upper, or top, electrode. One method of making these capacitors is to use a sacrificial layer along the sidewalls of a recess to form a space to remove the structural layer in which the capacitors are formed. Such use of sacrificial layers reduces the loss of oxide in the field outside of the array by accelerating the etching process of oxide materials within the array. A method of forming these sacrificial layers is described in U.S. patent application Ser. No. 10/714,115, which is incorporated by reference herein.
Formation of a Double-sided Container Capacitor Using a Sacrificial Layer
As pictured in
In
It should be appreciated that the first conductive layer 40 may be deposited using any one of a number of generally known deposition techniques without departing from the scope of the present teachings. The thickness of the lower electrode 40 can vary but preferably leaves room within the recess 12 for subsequent conformal capacitor dielectric and upper electrode layers. Preferably the lower electrode is between about 100 Å and 500 Å thick, more preferably between about 150 Å and 250 Å thick.
As shown in
The removal of the structural layer 10 (
The capacitor in
Sacrificial Layers
U.S. patent application Ser. No. 10/714,115, incorporated by reference above, describes the formation of double-sided container capacitors with a sacrificial layer. However, one problem with using sacrificial layers is that etching down a narrow capillary is difficult. The etch process can take a long time, exposing other exposed layers to the etchant in the meantime. Even if the selected etchant is very selective to the structural layer material and the lower electrode material, there will be some etching of the structural layer and the lower electrode. The etching of the lower electrode can cause poorly functioning capacitors. Substantial etching of the structural layer in the field regions outside the array can cause planarization problems in later processing steps.
Additionally, the materials for the sacrificial layer can interact with the lower electrode material. The selection of materials for the lower electrode and the sacrificial layer is preferably coordinated in order to minimize interaction between the two materials that could hinder the removal of the sacrificial layer.
Use of Enriched PSG as a Sacrificial Layer
In an embodiment shown in
In a preferred embodiment, the PSG 110 is made by pulsing the precursors in a CVD chamber. A process of depositing a doped oxide is described in U.S. Pat. No. 6,596,641, issued to Jost, et. al., the disclosure of which is herein incorporated by reference. While the '641 patent discusses forming BPSG, PSG can be similarly formed. In fact, an embodiment in the '641 patent describes forming the glass doped with as low as 0% boron, and up to 24% phosphorus. As described, a preferred set of precursors includes triethylphosphate (TEPO), TEOS, and ozone. Table 1 below illustrates one cycle of deposition in a preferred embodiment; the cycle can be repeated to attain the desired layer thickness.
TABLE 1
A preferred PSG deposition process
Step
Step
Step
Step
Step
Step
Step
Step
1
2
3
4
5
6
7
8
Step time
3 s
10 s
10 s
10 s
3 s
10 s
10 s
10 s
O3
off
off
on
off
off
off
on
off
TEPO
off
off
off
off
on
off
off
off
TEOS
on
off
off
off
off
off
off
off
In a preferred embodiment, the PSG layer 110 is covered by a thin protective layer 112, preferably undoped silicate glass (USG). Preferably, the USG layer 112 has a thickness of between about 10 Å and 30 Å, more preferably between about 15 Å and 25 Å. In
In
The lower electrode 120, as shown in
In
As shown in
Use of Germanium Oxide as a Sacrificial Layer
In another preferred embodiment, germanium oxide (GeOx) is used as the sacrificial liner. Germanium oxide can either be in the form of germanium (IV) oxide (GeO2) or germanium (II) oxide (GeO). Preferably the GeOx layer is between about 100 Å and 500 Å thick, more preferably between about 150 Å and 350 Å thick.
In a preferred embodiment, GeOx is formed with a high Ge percentage. The standard percentage of germanium in GeO2 is approximately 69% by weight. In a preferred embodiment, the germanium is at least 65% by weight of the GeOx. In a more preferred embodiment, the germanium in the GeOx is at least 70% by weight. A high content of germanium makes the sacrificial layer very etchable. In fact, with a sufficiently high germanium concentration, the GeO2 layer is water soluble. This allows for a wide variety of etchant possibilities because the sacrificial layer, and other exposed layers, would only need to be exposed to the etchant for a very limited time to remove the sacrificial material. Reducing the exposure time of neighboring layers to the etchant solution decreases the etching of surrounding materials, especially the lower electrode.
Because of its high instability, germanium oxide has traditionally not been grown and used in integrated circuit design. In this context, the germanium oxide need only exist for a limited period of time. In a preferred embodiment, the GeOx is grown in a CVD chamber. The germanium precursor is preferably an organometallic germanium compound or a germane (e.g. GeH4, Ge2H6, etc.). Perferably, the GeOx is formed from the reaction of germane (GeH4)and an oxygen source in a CVD chamber, particularly where the reactants are activated by plasma.
In a preferred embodiment, a very thin protective layer, preferably an oxide such as USG, is deposited over the GeOx layer in a similar fashion to the PSG layer discussed above. This will protect the GeOx layer from subsequent etch, CMP and wet clean steps, as described below. Preferably, the USG layer has a thickness of between about 10 Å and 30 Å, more preferably between about 15 Å and 25 Å. Because the USG layer is thin, it will preferably be etched away by the time the sacrificial layer is removed.
In a preferred embodiment, a polysilicon lower electrode is used with the germanium oxide sacrificial layer. Other conductive materials such as TiN, metals, and metal alloys can also be used as the lower electrode. A CMP step is preferably performed to level the surface of the lower electrode. In one embodiment, the GeOx and USG layers are then etched using aqueous HF with an HF concentration of between about 0.05 wt. % and 2.0 wt. %, more preferably between about 0.1 wt. % and 0.5 wt. %. The etching of the germanium oxide occurs at a temperature of between about 15° C. and 40° C., more preferably between about 20° C. and 25° C. The etch rate of the GeOx will be extremely high when using this chemistry. The structural layer, preferably comprising BPSG, is then removed by accessing three sides of the layer with a suitable BPSG etchant.
Referring now to
The lower electrode 320 is then formed within the annulus defined by the sacrificial layer 310 and protective liner 315, as shown in
The sacrificial layer 310 is removed, as shown in
As seen in
Use of Doped Oxides as Sacrificial Layers
In another preferred embodiment, a doped silicon oxide is used as the sacrificial layer. Preferably, the glass is borosilicate glass (BSG), phosphosilicate glass (PSG), or borophosphosilicate glass (BPSG), and the total dopant level by atomic percentage is preferably between about 5% and 15%, more preferably between about 8% and 12%. The described dopant levels by weight include the weight of both the phosphorus and the boron. These layers can also be formed by the process of the '641 patent to Jost, et al. Preferably the doped layer is between about 100 Å and 500 Å thick, more preferably between about 125 Å and 300 Å thick. When using this preferred embodiment, the structural layer is preferably a substantially undoped glass. Preferably, the level of dopants in the substantially undoped structural layer is less than about 3%, more preferably less than 2%. Examples of materials for the structural layer include spin-on glass (SOG) and PECVD SiO2.
It is known that doped glass can be etched selectively relative to substantially undoped glass. Preferably, the levels of dopants are selected that will produce good selectivity when etched by either HF vapor or wet chemistries such as acetic acid and HF. Gaseous HF etches doped oxides and leaves the undoped oxides substantially intact. In a preferred embodiment, an aqueous HF solution is used with an HF concentration of between about 0.5 wt. % and 15 wt. %, more preferably between about 2 wt. % and 10 wt. %. The substrate temperature is preferably between about 15° C. and 40° C., more preferably between about 20° C. and 25° C. When using these chemistries, the doped oxides within the mentioned ranges of dopant concentration can be etched selectively relative to the substantially undoped oxide structural layer 10 by magnitudes of up to 4,000 times selectivity.
In a preferred embodiment, a polysilicon lower electrode is used with the doped sacrificial layer. Other materials can also be used as the lower electrode, such as TiN, metals, or metal alloys. A CMP step is performed to level the surface of the lower electrode. Additionally, by removing the upper surface, the electrodes are electrically isolated from each other. Preferably, the sacrificial layer is then etched using aqueous HF. The preferably USG structural layer in the array is then isotropically removed by vapor etch or wet chemistries.
In
In
As seen in
Use of a Metal Nitride or Metal Oxide Sacrificial Layer
The use of a metal nitride or metal oxide sacrificial layer is described in detail in U.S. provisional patent Application No. 60/606,836, filed Sep. 1, 2004, entitiled “Method Of Obtaining Extreme Selectivity to Metal Nitrides and Metal Oxides” of Kevin R. Shea, Attorney docket No. MICRON.277PR, the disclosure of which is herein incorporated by reference. Exemplary lower electrode materials are polysilicon and titanium nitride (TiN). As discussed in the Shea application, 60/606,836 incorporated by reference above, the metal nitrides and metal oxides are preferably removed by using an ultra dilute or ultra buffered HF etchant. When using a metal nitride or metal oxide, such as HfN or Al2O3, occasionally the metals diffuse into the adjacent lower electrode. As described in the application, the etchant is extremely selective to the specified lower electrode materials. However, when the metals of the sacrificial layer diffuse into the lower electrode, they can cause the active species (primarily F− and some HF2−) of the etchant described in the Shea application, App. No. 60/606,836, to etch the lower electrode. The etching of the lower electrode can cause an increased rate of failures and increased production costs.
In order to solve the problem of lower electrode etching, metals of the sacrificial layer are preferably inhibited from diffusing into the lower electrode material. There are many materials which can be used to prevent interaction between the preferred materials when used as a protective liner between the sacrificial layer and the electrode. The protective liner is also preferably easily removed either when the sacrificial layer is removed, or when the structural layer is removed. In a preferred embodiment, doped and undoped silicon oxides are deposited in very thin layers in order to prevent interaction between the sacrificial layer and the electrode. Silicon oxide is easy to deposit as many tools are available for the deposition of oxide layers. In fact, some current production tools that deposit some of the preferred sacrificial materials (e.g. Al2O3 and other metal nitrides and metal oxides) can deposit an undoped or doped oxide layer after depositing the Al2O3.
Preferably, the protective liner is between about 10 Å and 40 Å, more preferably between about 15 Å and 25 Å. Preferred materials for the protective liner include USG, PSG, BSG, and BPSG. As the protective liner is preferably a doped or undoped silicon oxide, the layer will not be removed when the sacrificial layer is removed. The etchant used for the removal of the metal oxide or metal nitride layer is preferably very selective against the oxide of the structural layer. When the structural layer, preferably BPSG, is removed after the lower electrode is deposited, the oxide liner will also be removed by a selective oxide etch.
The removal of the sacrificial spacers is preferably performed by a HF solution having a low percentage of the H2F2 species of hydrogen fluoride. One form of such an etchant is an ultradilute HF solution. In a preferred embodiment, the ratio of water to HF is between about 1,000 to 1 and 10,000 to 1. Another embodiment of an etchant with a low percentage of the H2F2 species of hydrogen fluoride is an ultrabuffered solution. Preferably, the pH of such a solution is between about 3.5 and 5.5. More preferably, the pH of the buffered solution is between about 4.0 and 5.0. The wafer is preferably heated to a temperature of between about 50° C. and 90° C., more preferably between about 60° C. and 85° C.
An embodiment is illustrated in
Polysilicon Layer as a Sacrificial Layer
In another preferred embodiment, polysilicon is used as a sacrificial layer. In this embodiment, the lower electrode is preferably a metallic material, such as TiN, tungsten (W), ruthenium (Ru), or platinum (Pt). Many etchants are available for polysilicon that are selective to metallic materials which can be used as the lower electrode, and are also selective to materials that are used in the structural layer, typically a form of silicon oxide.
However, when using polysilicon sacrificial layers, it is difficult to control the etch process. For many processes it is desirable to retain a portion of the sacrificial layer so that the entirety of the container is not exposed or to avoid undesired etching of underlying materials. Polysilicon sacrificial layers, for example, could benefit from an etch stop in order to control the depth up to which the outside of the containers are exposed and to minimize risk that the underlying polysilicon plug gets damaged. Forming and controlling the etch stop layer can be done in several ways.
In a preferred embodiment, a collar is formed as a local source of dopant in the structural layer, which is preferably a form of oxide such as BPSG. The collar is preferably a heavily doped oxide layer, preferably BSG or PSG. The dopant of the oxide will diffuse into the poly sacrificial layer and cause a thin section of the sacrificial layer to be doped. The doped poly layer would have a different etch rate than the rest of the sacrificial layer, thus forming an etch stop layer. The skilled artisan will appreciate that such a collar can provide local doping as an etch stop for a variety of other sacrificial materials.
As shown in
In a preferred embodiment illustrated in
The dopant from the collar 603 will diffuse into the poly sacrificial layer 610 to form an etch stop layer 611. In
The sacrificial layer is etched by an etchant which etches undoped or low doped poly selective to doped poly. In a preferred embodiment where the collar 603 is BSG, the etch stop layer 611 will be a p-doped layer because boron is a p-type dopant. The poly sacrificial layer 610 can also be slightly n-doped in this embodiment. The non-p-doped portion of the poly sacrificial layer 610 can preferably be etched using “hot” TMAH (tetramethylammonium hydroxide). TMAH etches p-doped poly and other types of poly at substantially different rates. TMAH etches undoped poly at approximately 1 micron per minute, but etches p-doped doped poly at approximately 0.01 μm/min. Because of the difference in etch rates, the etch process can be stopped when the TMAH reaches the p-doped poly layer. In this preferred embodiment, the TMAH etch process is preformed at a temperature of between about 40° C. and 100° C., more preferably between about 50° C. and 70° C., with concentration levels of TMAH between about 1 wt. % and 25 wt. %, more preferably between about 5 wt. % and 25 wt. %.
When PSG is used as the collar, the phosphorus diffusing into the poly sacrificial layer makes the poly layer n-doped. However, TMAH and other ammonium based etchants do not respond well to n-doped etch stop layers unless they are very heavily doped. The difference in etch rates is generally much smaller for n-doped layers and substantially undoped poly than the difference in etch rates between p-doped layers and substantially undoped poly. Because of this p-doped etch stop layers are more preferred than n-doped etch stop layers.
In one embodiment, the structural layer 600 can then be removed faster than without using the sacrificial process flow using the space created by removing the sacrificial material above the etch stop layer.
In another embodiment shown in
Some of the metallic materials of the collar 703 create a risk of shorting the capacitors to one another. When the etch stop layer is reached in the etch process, the wet etch chemistry is changed to recess back the metallic collar 703 in order to prevent shorting.
In another embodiment seen in
The depth that the ions reach is determined by the energy (i.e. the velocity) of the ions. Concentration of the ions is controlled by the concentration of ions in the ion beam. Additionally, the concentration can be increased by multiple passes through the ion beam. Examples of preferable ion implantation tools include Applied Materials' (San Jose, Calif.) Quantum implanter and Axcelis' (Beverly, Mass.) HE Ion Implant Device.
Referring now to
As seen in
Expose portions of the implanted sacrificial layer 810 are preferably then etched away with an etchant that etches the implanted poly 810 selective to the poly which was not implanted 811. A preferred etchant is TMAH, with a concentration of between about 2 wt. % and 25 wt. %, more preferably between about 20 wt. % and 25 wt. %. Preferably, the temperature for the etch process is between about 20° C. and 100° C., more preferably between about 50° C. and 70° C. The unimplanted portion of the poly sacrificial layer acts as an etch stop for the etch process.
Intermediate and Final Structure
In a preferred embodiment shown in
These isolated lower electrodes will be ideally suited to the formation of a compact memory array. Preferred materials for the lower electrodes are polysilicon, TiN, metals, and metal alloys. Referring now to
Referring now to
The dimensions of the capacitor can relate to the performance of the DRAM memory cell array. With reference to
In a preferred embodiment illustrated in
In a preferred embodiment illustrated in
In a preferred embodiment illustrated in
These capacitors are preferably used in an array. For example,
In a preferred embodiment illustrated in
It will be appreciated by those skilled in the art that various omissions, additions and modifications may be made to the methods and structures described above without departing from the scope of the invention. All such modifications and changes are intended to fall within the scope of the invention, as defined by the appended claims.
Sandhu, Gurtej S., Shea, Kevin R., Torek, Kevin J., Hill, Chris W.
Patent | Priority | Assignee | Title |
10608096, | Jun 11 2018 | International Business Machines Corporation | Formation of air gap spacers for reducing parasitic capacitance |
10840349, | Jun 11 2018 | International Business Machines Corporation | Formation of air gap spacers for reducing parasitic capacitance |
10957778, | Jun 11 2018 | International Business Machines Corporation | Formation of air gap spacers for reducing parasitic capacitance |
11183577, | Jun 11 2018 | International Business Machines Corporation | Formation of air gap spacers for reducing parasitic capacitance |
8058126, | Feb 04 2009 | U S BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT | Semiconductor devices and structures including at least partially formed container capacitors and methods of forming the same |
8187934, | Jul 26 2005 | U S BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT | Reverse construction memory cell |
8692305, | Feb 04 2009 | U S BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT | Semiconductor devices and structures including at least partially formed container capacitors |
8871588, | Jul 26 2005 | U S BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT | Reverse construction integrated circuit |
Patent | Priority | Assignee | Title |
5278091, | May 04 1993 | Micron Technology Inc | Process to manufacture crown stacked capacitor structures with HSG-rugged polysilicon on all sides of the storage node |
5354705, | Sep 15 1993 | Micron Technology Inc | Technique to fabricate a container structure with rough inner and outer surfaces |
5937294, | Aug 11 1995 | Micron Technology, Inc. | Method for making a container capacitor with increased surface area |
5956587, | Feb 17 1998 | TAIWAN SEMICONDUCTOR MANUFACTURING CO , LTD | Method for crown type capacitor in dynamic random access memory |
6180450, | Apr 07 1993 | Round Rock Research, LLC | Semiconductor processing methods of forming stacked capacitors |
6312986, | Aug 19 1998 | Micron Technology Inc. | Concentric container fin capacitor and method |
6350647, | Nov 09 1998 | NEC Electronics Corporation | Semiconductor memory device and manufacturing method of the same |
6372574, | Jun 02 2000 | CONVERSANT INTELLECTUAL PROPERTY MANAGEMENT INC | Method of forming a capacitor container electrode and method of patterning a metal layer by selectively silicizing the electrode or metal layer and removing the silicized portion |
6451661, | Jun 03 1998 | Round Rock Research, LLC | DRAM capacitor formulation using a double-sided electrode |
6451667, | Dec 21 2000 | Infineon Technologies AG | Self-aligned double-sided vertical MIMcap |
6458652, | Aug 20 2001 | Round Rock Research, LLC | Methods of forming capacitor electrodes |
6507064, | May 10 2000 | U S BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT | Double sided container capacitor for DRAM cell array and method of forming same |
6524912, | Aug 31 2000 | Micron Technology, Inc. | Planarization of metal container structures |
6569689, | Mar 01 1999 | Round Rock Research, LLC | Method of forming a capacitor |
6596641, | Mar 01 2001 | Micron Technology, Inc. | Chemical vapor deposition methods |
6635547, | Jun 03 1998 | Round Rock Research, LLC | DRAM capacitor formulation using a double-sided electrode |
6667209, | Feb 08 2002 | Samsung Electronics Co., Ltd. | Methods for forming semiconductor device capacitors that include an adhesive spacer that ensures stable operation |
20020168830, | |||
20030001268, | |||
20050250339, |
Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
Dec 10 2004 | HILL, CHRIS W | Micron Technology, Inc | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 016129 | /0975 | |
Dec 10 2004 | SHEA, KEVIN R | Micron Technology, Inc | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 016129 | /0975 | |
Dec 20 2004 | TOREK, KEVIN J | Micron Technology, Inc | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 016129 | /0975 | |
Dec 20 2004 | SANDHU, GURTEJ S | Micron Technology, Inc | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 016129 | /0975 | |
Dec 22 2004 | Micron Technology, Inc. | (assignment on the face of the patent) | / | |||
Apr 26 2016 | Micron Technology, Inc | U S BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT | SECURITY INTEREST SEE DOCUMENT FOR DETAILS | 038669 | /0001 | |
Apr 26 2016 | Micron Technology, Inc | MORGAN STANLEY SENIOR FUNDING, INC , AS COLLATERAL AGENT | PATENT SECURITY AGREEMENT | 038954 | /0001 | |
Apr 26 2016 | Micron Technology, Inc | U S BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT | CORRECTIVE ASSIGNMENT TO CORRECT THE REPLACE ERRONEOUSLY FILED PATENT #7358718 WITH THE CORRECT PATENT #7358178 PREVIOUSLY RECORDED ON REEL 038669 FRAME 0001 ASSIGNOR S HEREBY CONFIRMS THE SECURITY INTEREST | 043079 | /0001 | |
Jun 29 2018 | U S BANK NATIONAL ASSOCIATION, AS COLLATERAL AGENT | Micron Technology, Inc | RELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS | 047243 | /0001 | |
Jul 03 2018 | MICRON SEMICONDUCTOR PRODUCTS, INC | JPMORGAN CHASE BANK, N A , AS COLLATERAL AGENT | SECURITY INTEREST SEE DOCUMENT FOR DETAILS | 047540 | /0001 | |
Jul 03 2018 | Micron Technology, Inc | JPMORGAN CHASE BANK, N A , AS COLLATERAL AGENT | SECURITY INTEREST SEE DOCUMENT FOR DETAILS | 047540 | /0001 | |
Jul 31 2019 | JPMORGAN CHASE BANK, N A , AS COLLATERAL AGENT | MICRON SEMICONDUCTOR PRODUCTS, INC | RELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS | 051028 | /0001 | |
Jul 31 2019 | MORGAN STANLEY SENIOR FUNDING, INC , AS COLLATERAL AGENT | Micron Technology, Inc | RELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS | 050937 | /0001 | |
Jul 31 2019 | JPMORGAN CHASE BANK, N A , AS COLLATERAL AGENT | Micron Technology, Inc | RELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS | 051028 | /0001 |
Date | Maintenance Fee Events |
Mar 25 2008 | ASPN: Payor Number Assigned. |
Mar 25 2008 | RMPN: Payer Number De-assigned. |
Jul 13 2011 | M1551: Payment of Maintenance Fee, 4th Year, Large Entity. |
Oct 23 2012 | ASPN: Payor Number Assigned. |
Oct 23 2012 | RMPN: Payer Number De-assigned. |
Jul 29 2015 | M1552: Payment of Maintenance Fee, 8th Year, Large Entity. |
Aug 05 2019 | M1553: Payment of Maintenance Fee, 12th Year, Large Entity. |
Date | Maintenance Schedule |
Feb 12 2011 | 4 years fee payment window open |
Aug 12 2011 | 6 months grace period start (w surcharge) |
Feb 12 2012 | patent expiry (for year 4) |
Feb 12 2014 | 2 years to revive unintentionally abandoned end. (for year 4) |
Feb 12 2015 | 8 years fee payment window open |
Aug 12 2015 | 6 months grace period start (w surcharge) |
Feb 12 2016 | patent expiry (for year 8) |
Feb 12 2018 | 2 years to revive unintentionally abandoned end. (for year 8) |
Feb 12 2019 | 12 years fee payment window open |
Aug 12 2019 | 6 months grace period start (w surcharge) |
Feb 12 2020 | patent expiry (for year 12) |
Feb 12 2022 | 2 years to revive unintentionally abandoned end. (for year 12) |